The Striegler Lab

Home

Research

Lab members

Publications

on tour...

Contributions to Peer-Reviewed Journals and Books

• S. Striegler,* Selective hydrolysis of heterooligosaccharides by poly(acrylate) gel catalysts ACS Catal. 2024, 14 (22), 16723-16730.

• S. Striegler,* Developing catalysts for the hydrolysis of glycosidic bonds in oligosaccharides using a spectrophotometric screening assay ACS Catal. 2024, 14 (17), 12940-12946.

• B. Sharma, S. Striegler,* Nanogel catalysts for the hydrolysis of underivatized disaccharides identified by a fast screening assay ACS Catal. 2023, 13 (3), 1614-1620.

• J. R. DeMoulpied, J. A. Killenbeck, Z. G. Schichtl, B. Sharma, S. Striegler, R. H. Coridan,* Characterizing the Solvent-Induced Inversion of Colloidal Aggregation During Electrophoretic Deposition Adv. Mater. Interfaces 2022, 2201779 .

• B. Sharma, S. Striegler,* Polarity and critical micelle concentration of surfactants support the catalytic efficiency of nanogels during glycoside hydrolyses ACS Catal. 2022, 12(15), 8841-8847.

• S. Striegler,* I. Orizu, Solvent-controlled synthesis of bulky and polar-bulky galactonoamidines Carb. Res. 2022, 513 , 108520.

• C. M. Clem, B. Sharma, S. Striegler,* Structure-activity-relationship studies to elucidate sources of antibacterial activity of modular polyacrylate microgels ACS Appl. Bio Mater. 2021, 4, 10, 7578-7586.

• S. Striegler,* B. Sharma, I. Orizu, Microgel-catalyzed hydrolysis of non-activated disaccharides ACS Catal. 2020, 10(24), 14451-14456.

• B. Sharma, C. M. Clem, A. Diaz Perez, S. Striegler,* Antimicrobial activity of microgels with immobilized copper(II) complex linked to crosslinking and composition ACS Appl. Bio Mater. 2020, 3(11), 7611-7619.

• B. Sharma, S. Striegler,* Nonionic surfactant blends to control the size of microgels and their catalytic performance during glycoside hydrolyses ACS Catal. 2020, 10(16), 9458-9463.

• B. Sharma, S. Striegler,* Tailored interactions of the secondary coordination sphere enhance the hydrolytic activity of crosslinked microgels ACS Catal. 2019, 9(3), 1686-1691.

• B. Sharma, J.B. Pickens, S. Striegler,* J.D. Barnett, Biomimetic glycoside hydrolysis by a microgel templated with a competitive glycosidase inhibitor ACS Catal. 2018, 8(8), 8788-8795.

• B. Sharma, S. Striegler,* M. Whaley, Modulating the catalytic performance of an immobilized catalyst with matrix effects - a critical evaluation ACS Catal. 2018, 8(8), 7710-7718.

• B. Sharma, S. Striegler,* Crosslinked microgels as platform for hydrolytic catalysts Biomacromolecules 2018, 19(4), 1164-1174.

• J.B. Pickens, L.G. Mills, F. Wang,* S. Striegler,* Evaluating hydrophobic galactonoamidines as transition state analogs for enzymatic β-galactoside hydrolysis Biorg. Chem. 2018, 77, 144-151.

• J.B. Pickens, F. Wang, S. Striegler,* Picomolar inhibition of β-galactosidase (bovine liver) attributed to loop closure Biomol. Med. Chem. 2017, 25(20), 5194-5202.

• S. Striegler,* J.B. Pickens, Discrimination of chiral copper(II) complexes upon binding of galactonoamidine ligands Dalton Trans. 2016. 45, 15203-15210.

• J.B. Pickens, S. Striegler,* Q.-H. Fan, Arabinoamidine synthesis and its inhibition toward β-glucosidase (sweet almonds) in comparison to a library of galactonoamidines Biomol. Med. Chem. 2016, 24(16), 3371-3377.

• S. Striegler,* Q.-H. Fan, N. P. Rath, Binuclear copper(II) complexes discriminating epimeric glycosides and α- and β-glycosidic bonds in aqueous solution, J. catal. 2016. 338, 349-364.

• Q.-H. Fan, J. B. Pickens, S. Striegler,* Cedric D. Gervaise, Illuminating the binding interactions of galactonoamidines during the inhibition of β-galactosidase (E. Coli), Bioorg. Med. Chem. 2016. 24, 661-671.

• Q.-H. Fan, K. A. Claunch, S. Striegler,* Structure-activity relationship of highly potent galactonoamidine inhibitors toward β-galactosidase (A. oryzae), J. Med. Chem. 2014. 57 (21) , 8999-9009

• Q.-H. Fan, S. Striegler*, R.G. Langston and J.D. Barnett, Evaluating N-benzylgalactonoamidines as putative transition state analogs for β-galactoside hydrolysis, Org. Biomol. Chem. 2014, 12(17) 2792-2800.

• J.D. Barnett, S. Striegler,* Tuning templated microgel catalysts for selective glycoside hydrolysis, Top. Catal. 2012, 55(7) , 460-465.

• R. Kanso, E.A. Yancey, S. Striegler,* N-benzylgalactonoamidines as potent β-galactosidase inhibitors, Tetrahedron 2012, 68(1), 47-52.

• S. Striegler,* J.D. Barnett and N.A. Dunaway, Glycoside hydrolysis with sugar-templated microgel catalysts, ACS catal. 2012, 2(1), 50-55.

• S. Striegler,* M. Dittel, R. Kanso, N.A. Alonso and E.C. Duin, Hydrolysis of glycosides with microgel catalysts, Inorg. Chem. 2011, 50(18), 8869-8878.

• R. Kanso, S. Striegler,* Multi gram-scale synthesis of galactothionolactam and its transformation into a galactonoamidine, Carbohydr. Res. 2011, 346(7), 897-904.

• S. Striegler,* N.A. Dunaway, M.G. Gichinga, L.K. Milton, Binuclear complexes for aerobic oxidation of primary alcohols and carbohydrates, Tetrahedron 2010, 66(40), 7927-7932.

• S. Striegler*, N.A. Dunaway, M.G. Gichinga, J.D. Barnett and A.-G.D. Nelson, Evaluating binuclear copper(II) complexes for glycoside hydrolysis, Inorg. Chem. 2010, 49(6), 2639-2648.

• M.G. Gichinga, S. Striegler*, N.A. Dunaway and J.D. Barnett, Miniemulsion polymers as solid support for transition metal catalysts, Polymer 2010, 51(3), 606-615.

Selected publications before 2010

• S. Striegler,* M.G. Gichinga, Disaccharide recognition by binuclear copper(II) complexes, Chem. Commun. 2008 , 5930-5932 .

• M.G. Gichinga, S. Striegler,* Effect of water on the catalytic oxidation of catechols, J. Am. Chem. Soc. 2008, 130(15), 5150-5156 .

• S. Striegler,* M.G. Gichinga, M. Dittel, Macromolecular salen catalyst with largely enhanced catalytic activity, Org. Lett. 2008, 10(2), 241-244; highlighted by Y. Uozumi, T. Osako in SYNFACTS 2008, 4, 0438.

• S. Striegler,* M. Dittel, A sugar discriminating binuclear copper(II) complex, J. Am. Chem. Soc. 2003, 125(38), 11518-11524.

• S. Striegler,* E. Tewes, Investigation of sugar binding sites in ternary ligand–copper(II)–carbohydrate complexes, Eur. J. Inorg. Chem. 2002, 2, 487-495.